(Q60689129)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20624498%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome (English)

1 reference

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7 February 2020

1 reference

7

1 reference

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7 February 2020

Manfred Stuhrmann

14

1 reference

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7 February 2020

10

Gudrun Göhring

1 reference

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7 February 2020

author name string

Kathrin Wessels

1

1 reference

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7 February 2020

Bettina Bohnhorst

2

1 reference

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7 February 2020

Ingrid Luhmer

3

1 reference

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7 February 2020

Susanne Morlot

4

1 reference

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7 February 2020

Axel Bohring

5

1 reference

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7 February 2020

Jon Jonasson

6

1 reference

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7 February 2020

Dorothea Gadzicki

8

1 reference

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7 February 2020

Stefanie Glaser

9

1 reference

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7 February 2020

Madeleine Mälzer

11

1 reference

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7 February 2020

Anke Hein

12

1 reference

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7 February 2020

Mine Arslan-Kirchner

13

1 reference

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7 February 2020

Jörg Schmidtke

15

1 reference

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7 February 2020

Brigitte Pabst

16

1 reference

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7 February 2020

publication date

30 July 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20624498%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Medical Genetics

7 February 2020

published in

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7 February 2020

volume

53

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7 February 2020

issue

5

1 reference

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7 February 2020

page(s)

280-285

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20624498%20AND%20SRC:MED&resulttype=core&format=json

Identification of multiple distinct Snf2 subfamilies with conserved structural motifs.

7 February 2020

cites work

1 reference

2 April 2022

https://opencitations.net/index/coci/api/v1/citations/10.1093/NAR/GKL295

Identifiers

DOI

10.1016/J.EJMG.2010.07.002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20624498%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference